Gene: AGT ×
Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs699
rs699
AGT
134 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.070 0.714 7 1999 2014
dbSNP: rs3789678
rs3789678
AGT
5 1.000 0.040 1 230713736 intron variant C/T snv 0.15 0.010 1.000 1 2015 2015
dbSNP: rs4762
rs4762
AGT
35 0.637 0.440 1 230710231 missense variant G/A snv 0.12 0.11 0.010 1.000 1 2016 2016
dbSNP: rs7539020
rs7539020
AGT
3 1.000 0.040 1 230713444 intron variant C/T snv 0.43 0.010 1.000 1 2015 2015